EP3371335B1 - Festschmierstoffbeschichtete stahlartikel, verfahren und vorrichtung zu deren herstellung und bei der herstellung verwendetes abschrecköl - Google Patents

Festschmierstoffbeschichtete stahlartikel, verfahren und vorrichtung zu deren herstellung und bei der herstellung verwendetes abschrecköl Download PDF

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Publication number
EP3371335B1
EP3371335B1 EP16862557.2A EP16862557A EP3371335B1 EP 3371335 B1 EP3371335 B1 EP 3371335B1 EP 16862557 A EP16862557 A EP 16862557A EP 3371335 B1 EP3371335 B1 EP 3371335B1
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Prior art keywords
quenching
nitriding
steel
oil
nitrided
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EP16862557.2A
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English (en)
French (fr)
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EP3371335A1 (de
EP3371335A4 (de
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Mikael Berg
Mikael FÄLLSTRÖM
Boris Zhmud
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Tribonex AB
Bodycote Varmebehandling AB
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Tribonex AB
Bodycote Varmebehandling AB
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    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/56—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering characterised by the quenching agents
    • C21D1/58—Oils
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/06—Surface hardening
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
    • C23C8/08—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
    • C23C8/24—Nitriding
    • C23C8/26—Nitriding of ferrous surfaces
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/40—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions
    • C23C8/42—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions only one element being applied
    • C23C8/48—Nitriding
    • C23C8/50—Nitriding of ferrous surfaces
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/80—After-treatment
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/106—Naphthenic fractions
    • C10M2203/1065—Naphthenic fractions used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
    • C10M2227/065—Organic compounds derived from inorganic acids or metal salts derived from Ti or Zr
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
    • C10M2227/066—Organic compounds derived from inorganic acids or metal salts derived from Mo or W
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/09—Complexes with metals
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/20—Metal working
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/40—Generators or electric motors in oil or gas winning field

Definitions

  • the present invention relates in general to manufacturing of lubricant-coated steel articles, and in particular to nitrided lubricant-coated steel articles.
  • Nitriding is a heat treating process that diffuses nitrogen into the surface of a metal to create a case hardened surface. Nitriding is most commonly used on low-carbon, low-alloy steels, however, during recent years, also higher alloyed steels have been nitrided with advantageous results.
  • the main nitriding methods used today are: gas nitriding, salt bath nitriding, and plasma nitriding, which are named after the medium used to donate nitrogen.
  • Nitriding typically imparts a high surface hardness which promotes high resistance to wear, scuffing, galling and seizure. Fatigue strength is increased mainly by the development of surface compressive stresses.
  • Nitriding is often performed at elevated temperature and is therefore typically ended by a cooling or quenching step in which the steel product is cooled down.
  • Fast quenching after nitriding will increase the solution hardening effect from the entrapped nitrogen but this effect is proportionally small compared to the precipitation hardening effect derived from the formation of hard nitrides between alloying elements and nitrogen in the steel surface.
  • Alloying elements such as Cr, Al, V, Ti and Mo forms hard nitrides in steel during nitriding and the level of such alloying elements in the steel has a huge impact on the nitriding result in terms of hardness, wear resistance and fatigue strength.
  • Quenching oils and heat treatment fluids are designed for rapid or at least controlled cooling of steel or other metals as part of a hardening, tempering or other heat-treating process, such as nitriding.
  • Typical applications include gears, crankshafts, camshafts, racks, pinions, axles, races, drive shafts, center pins, cylinder blocks for hydraulic motors, vanes for pumps, piston skirts, chain components, slideways, cam followers, valve parts, extruder screws, die-casting tools, forging dies, extrusion dies, firearm components, injectors, plastic-mold tools, conveyor guides, etc.
  • nitrided materials Due to the typical beneficial properties of nitrided materials, they are often used in applications where the surfaces are exposed to mechanical contact with other solid or liquid objects, in particular, in moving contacts. In such applications, low friction and wear resistance are of interest. Lubrication is the standard way to address friction and wear problems. Depending on application, liquid and/or solid lubricants can be used. Liquid lubricants are the preferred choice when long service life, serviceability, corrosion protection, cleaning and cooling are all important. Solid lubricants are used in special cases where the use of liquid lubricants is not an option, due, for instance, to thermal conditions or surrounding environment. Solid lubricants are especially effective in controlling wear in highly loaded sliding contacts and hence are often used in applications being exposed to wear.
  • thermoset, UV-set or oxidation-drying polymer binder is used to retain the solid lubricant on the surface.
  • the surface has first to be cleaned, then coated in a separate step, and then finally cured.
  • heating and/or mechanical treatment and/or cleaning may influence the composition and properties of the surface of the nitrided object itself.
  • Heating at a low nitrogen potential may e.g. cause de-nitriding of the objects surface and heat treatment and mechanical interaction may alter texture, hardness, etc. of the nitrided object.
  • PVD physical vapor deposition
  • PA-CVD plasma-assisted chemical vapor deposition
  • Similar vacuum processes whereby solid lubricants are embedded into a hard coating - such as diamond-like carbon - matrix.
  • This technology is used, in particular, to manufacture products such as Balinit C (Oerlikon), MoST (Teer Coatings) and others.
  • Balinit C Olelikon
  • MoST Teer Coatings
  • Nitrided steel articles can also be CVD coated by certain solid lubricants in a separate processing step. This might produce a tribological effect. For instance, one might produce MoS 2 and WS 2 coating by a CVD process reacting volatile metal carbonyl complexes, Mo(CO) 6 and W(CO) 6 , with mercaptanes or organic sulfides, such as dimethylsulfides. Unfortunately, coatings so produced often tend to be fluffy and exhibit poor adhesion to the substrate. Possible reasons may be found in contamination or gas adsorption on the nitrided surface before coating or in surface modifications during cleaning procedures.
  • a gas nitrocarburizing treatment which produces a compound layer mainly composed of epsilon iron nitride.
  • a heat treatment in 570-580°C in a carbonitriding gas atmosphere forms a nitrogen diffusion layer.
  • a treatment in an oxidizing atmosphere at 450-500°C forms an oxide layer.
  • the oxide layer is laminated on the compound layer, giving an improved wear and corrosion resistance.
  • a general object of the present invention is to provide solid lubricant-coated nitrided steel articles with enhanced tribological properties.
  • a method for manufacturing of steel articles comprises nitriding a steel article at a nitrification temperature in the interval 350-650°C.
  • the nitriding of a steel article results in a nitrided steel article.
  • the nitrided steel article is quenched in a reactive quenching oil from the nitrification temperature.
  • the reactive quenching oil contains one or more surface-reactive compounds serving as carriers of at least one of S, P, B, Mo and W.
  • the quenching additionally comprises coating of the nitrided steel article by a solid lubricant comprising at least one of S, P, B, Mo and W.
  • the reactive quenching oil comprises at least 0.1% of weight and at most 10% of weight of the total of S, P, B, Mo and W.
  • the nitrided steel article is maintained in an atmosphere of a nitrogen potential prohibiting de-nitriding an entire time between the nitriding and the quenching.
  • One advantage with the proposed invention is that it results in solid lubricant coated nitrided steel articles with controlled surface properties and enhanced tribological performance. Furthermore, the solid lubricant coated nitrided steel articles are produced in an economical and non-complex process. Other advantages will be appreciated when reading the detailed description.
  • Nitriding processes are thermochemical processes that at an elevated temperature provides nitrogen or alternatively both nitrogen and carbon to a steel surface with the purpose to generate a hardened surface layer.
  • the surface layer comprises either a diffusion zone and a compound zone or alternatively only a diffusion zone.
  • the compound zone is a phase transitioned layer comprising nitrides. At higher temperatures, also an austenitic or a martensitic zone may be present.
  • the thermochemical nitriding process can be performed in a gas atmosphere, in a salt bath or by a plasma process. Such processes can be denoted as gas nitriding, gas nitrocarburization, salt bath nitriding, salt bath nitrocarburization, plasma nitriding and plasma nitrocarburization.
  • the nitriding process may be proceeded by a pre-oxidation in the temperature interval of 300-400°C during 0.5 - 3 hours.
  • the work piece to be nitrided is placed in a chamber filled with a donor gas at a high temperature.
  • the donor is usually ammonia, which is why it is sometimes known as ammonia nitriding.
  • ammonia comes into contact with the heated work piece it disassociates into nitrogen and hydrogen. The nitrogen then diffuses onto the surface of the material creating a nitride layer.
  • the nitrogen donating medium is a nitrogen-containing salt such as cyanide salt.
  • nitrogen is diffused into the surface of a metal at sub-critical temperatures at ferritic stage to create a case hardened surface.
  • the salts are also used to donate carbon to the workpiece surface, hence the salt bath process is also known as a nitrocarburizing process.
  • the temperature used in all nitrocarburizing processes is 550-570°C.
  • Plasma nitriding also known as ion nitriding, plasma ion nitriding or glow-discharge nitriding
  • ion nitriding plasma ion nitriding or glow-discharge nitriding
  • thermochemical treatment which is carried out in a mixture of nitrogen, hydrogen, and an optional carbon spending gas in the case of nitrocarburizing.
  • a glow discharge with a high ionization level is generated around the parts placed in a reaction chamber. As a result, nitrogen-rich nitrides are formed at the surface.
  • Plasma nitriding allows modification of the surface according to the desired properties. Tailor made layers and hardness profiles can be achieved by adapting the gas mixture: from a compound layer-free surface with low nitrogen contents up to 500 microns thick, to a compound layer with high nitrogen contents and an add-on of carbonic gas (plasma nitrocarburation).
  • the wide applicable temperature range enables a multitude of applications, beyond the possibilities of gas or salt bath processes.
  • Plasma nitriding efficiency does not primarily depend on the temperature. Plasma nitriding can thus be performed in a broad temperature range, from 260 °C to more than 600 °C. For instance, at moderate temperatures, stainless steels can be nitrided without the formation of chromium nitride precipitates and will hence maintain their corrosion resistance properties.
  • Plasma nitriding is a smart choice whenever parts are required to have both nitrided and soft areas.
  • Typical applications include gears, crankshafts, camshafts, cam followers, valve parts, extruder screws, pressure-die-casting tools, forging dies, cold forming tools, injectors and plastic-mould tools, long shafts, axis, clutch and engine parts.
  • Plasma nitriding and plasma nitrocarburising are often preferred to the corresponding gas processes if masking is required.
  • a diffusion zone is a nitrogen influenced surface layer where incorporated nitrogen influences the hardness of the steel by solution hardening and precipitation hardening.
  • a compound zone is a phase-transitioned surface layer comprising iron nitrides ( ⁇ '-nitride and/or ⁇ -nitride), carbonitrides and nitrides with alloying elements of the steel.
  • All iron based steel materials can be treated by a nitriding process, comprising but not limited to carbon steels, low-alloyed steels, engineering steels, hardening and temper steels, case hardened steels, tool steel, stainless steel, precipitation hardening steels/Stainless steels and other steel variants.
  • Quenching oil and heat treatment fluids are designed for rapid or controlled cooling of steel or other metals as part of a hardening, tempering or other heat-treating process, such as nitriding.
  • Quench oil serves two primary functions. It facilitates hardening of steel by controlling heat transfer during quenching, and it enhances wetting of steel during quenching to minimize the formation of undesirable thermal and transformational gradients which may lead to increased distortion and cracking.
  • the quenching oil should have ability to deliver constant quenching performance and cooling speed.
  • the quenching oil also preferably presents ability to withstand high thermal shocks.
  • the quenching oil should also provide oxidation resistance, of ingredients of the oil as well as to the quenched work piece.
  • the quenching oil should also be selected to give a good surface cleanliness and no deformation of hardened castings.
  • the invention presented in the present disclosure instead utilizes heat-induced deposition of solid lubricants onto a nitrided surface.
  • the temperatures at which typical nitriding processes are performed are high enough also to initiate solid lubricant formation.
  • difficulties to provide suitable components of the solid lubricant into the nitriding chamber itself makes a direct coating troublesome.
  • the present invention focusses on the last process in which the high temperatures are involved - the quenching.
  • a reactive quenching oil hardening/quenching can be combined with deposition of a solid lubricant film.
  • the only heat source used to trigger the chemical reaction is the heat retained by steel parts after the nitriding step. During the nitriding, the parts are typically heated up to 350-650°C. This temperature is high enough to initiate a reaction with specific EP/AW additives present in the quenching oil.
  • the reactive quenching oil contains one or more surface-reactive compounds serving as carriers of at least one of the following chemical elements: S, P, B, Mo and W.
  • the overall cooling speed in the reactive quenching process is similar to that for a regular quenching process, topping to 50-250°C/s, and therefore, the overall quench time and hardness of the treated parts will be identical to a non-reactive quenching processes.
  • the reactive quenching additionally comprises coating, in the course of the quench operation, of the nitrided steel article by a solid lubricant, containing at least one of the following chemical elements: S, P, B, Mo and W in its chemical composition.
  • a solid lubricant containing at least one of the following chemical elements: S, P, B, Mo and W in its chemical composition.
  • Steel parts which underwent reactive quenching exhibit the presence of a solid lubricant film, more than 0.1 ⁇ m thick, composed of specific chemical elements originally present in the additive package. This will be discussed further in a few examples below.
  • the solid lubricant is chemically bonded directly to a portion of the nitride layer that has a highest nitrogen content. Furthermore, if no oxygen is allowed to reach the nitrided work piece, except where included in the nitriding process, the bond between the solid lubricant and the nitride layer becomes essentially oxygen-free, which typically enhance the bonding strength.
  • Fig. 1 illustrates an example of a typical cooling curve 301.
  • the curve 300 illustrates the cooling rate.
  • a hot metal piece is immersed into the oil, a vapor layer near the metal surface is momentarily generated due to oil boiling or thermal degradation.
  • the properties of the vapor layer depend on the base oil type and surface-active additives used in the quench oil formulation. As long as such a vapor blanket is there, the cooling rate is relatively slow because the vapor layer acts as a thermal insulator.
  • a typical cooling rate could be around 20-40°C/s.
  • nucleate boiling stage B Nucleate boiling begins when the surface temperature drops to the point where the vapor layer becomes unstable and bubble formation occurs due to boiling. This stage exhibits the greatest heat transfer rates of the overall quench cooling process, and may reach 50-250°C/s. It is at this stage that the surface reaction with EP/AW additives present in the reactive quench oil is initiated. Accordingly, light base oils with low boiling temperatures are better suited for use in combination with more reactive additives, such as phosphates, while heavy base oils with high boiling temperature are better suited for use in combination with less reactive additives, such as sulfides.
  • C-stage convective cooling
  • the cooling intensity depends on oil viscosity, with lower viscosities enabling more rapid cooling.
  • the quench process illustrated in Fig. 1 should be understood as an example of a general quench process.
  • the actual numbers for the cooling rates at the different stages may vary depending on the actual content. Some of this will be discussed more in detail further below. However, the art of modifying cooling rates is, as such, well known in prior art.
  • Fig. 2 illustrates a flow diagram of steps of an embodiment of a method for manufacturing of steel article.
  • the process starts in step 200.
  • a steel article is nitrided at a nitrification temperature in the interval 350-650°C. This nitriding results in a nitrided steel article.
  • the nitrided steel article is quenched in a reactive quenching oil from the nitrification temperature.
  • the reactive quenching oil comprises at least one of S, P, B, Mo and W.
  • the step of quenching 220 additionally comprises the step 222 of coating of the nitrided steel article by a solid lubricant comprising at least one of S, P, B, Mo and W.
  • a solid lubricant comprising at least one of S, P, B, Mo and W.
  • the reactive quenching oil comprises S and at least one of Mo and W.
  • the reactive quenching oil preferably comprises at least 0.1% of weight of the doping elements, such as e.g. S, P, B, Mo and/or W.
  • the doping elements such as e.g. S, P, B, Mo and/or W.
  • Increasing the additive treat levels speeds up deposition of solid lubricant yet increases the cost for shorter quench oil service life and thus increases operational costs.
  • the quenching step is performed directly in connection with the end of the nitriding step.
  • no diffusion or other time-dependent effects may influence the result of the nitriding and since the nitriding atmosphere prohibits unwanted substances to reach the surface of the steel article, a "clean" surface on which the solid lubricant coating is to be performed can be ensured.
  • the nitrided steel article is maintained in a clean atmosphere with a high nitrogen potential an entire time between the step of nitriding and the step of quenching, and even more preferably if the atmosphere presents a nitrogen potential that is high enough to prevent de-nitriding of the surface of the nitrided steel article.
  • the nitrided steel article is maintained at the nitrification temperature an entire time between the step of nitriding and the step of quenching.
  • the nitriding step is performed according to the Corr-I-Dur ® process.
  • Corr-I-Dur ® is a thermochemical treatment, proprietary for Bodycote, for simultaneous improvement of corrosion resistance and wear properties through generating an iron nitride-oxide compound layer.
  • Corr-I-Dur ® treatment involves a combination of various low temperature thermochemical process steps, mainly gaseous nitrocarburizing and oxidizing. In the process, a boundary layer consisting of three zones is produced. The diffusion layer forms the transition to the substrate and consists of interstitially dissolved nitrogen and nitride precipitations which increase the hardness and the fatigue strength of the component.
  • a carbonitride mainly of the hexagonal epsilon phase Towards the surface it is followed by the compound layer, a carbonitride mainly of the hexagonal epsilon phase.
  • the Fe 3 O 4 iron oxide (magnetite) in the outer zone takes the effect of a passive layer comparable to the chromium-oxides on corrosion resistant steels. Due to the less metallic character of oxide and compound layer and the high hardness abrasion, adhesion and seizing wear can be distinctly reduced. Corr-I-Dur ® has very little effect on distortion and dimensional changes of components compared to higher temperature case hardening processes.
  • Corr-I-Dur ® Typical applications include brake pistons, ball joints, pump covers, wiper axis, differential axis, selector shafts, bolts, bushings and fastener elements for automotive applications. Also, hydraulic pistons and housings, several axis and shafts for general industry use. Especially, fill chambers and casting dies in aluminium die casting processes get benefit by the low reactivity between molten metal and the Corr-I-Dur ® surface. Corr-I-Dur ® can be applied to nearly all plain and low alloyed ferrous materials as case hardening, heat treatable, cold forming and easy machining steel.
  • heat treatment furnaces equipped to provide a protecting and controlled atmosphere during both heating and cooling have been used.
  • a steel of the type SS2172 was used in this particular embodiment.
  • the process started with a preheating and pre-oxidation at 400°C for about 1-2 hours in air. This pre-oxidation is performed to ensure an even nitrocarburizing result for this steel.
  • This is schematically illustrated in Fig. 3 .
  • a gas mixture of 35 % ammonia (NH 3 ), 5 % carbon dioxide (CO 2 ) and 60 % nitrogen gas (N 2 ) was used, measure in % by volume.
  • the nitrocarburizing was performed at 580°C.
  • the total gas flow corresponded to 3.5 times the volume of the furnace per hour.
  • This total gas flow influences the nitrogen activity, but is dependent on furnace and has typically to be adapted for each furnace type.
  • the nitrogen activity, a N during the nitrocarburizing step varied between 2.5 and 5, however, according to earlier experience, nitrogen activities in the range of 0.2 to 20 are possible to use for creating requested results.
  • a nitrided layer with a compound layer is the goal, which requires a concentration of nitrogen in the surface of at least 6% by weight.
  • the type of compound zone that was achieved and studied for this particular embodiment has a composition of pure ⁇ nitride or a mixture between ⁇ nitride and ⁇ ' nitride. These particular experiments gave a nitrocarburizing layer with a compound zone thickness of 10-25 ⁇ m.
  • the quenching is performed in a cooling chamber directly connected to the nitrocarburizing furnace.
  • the atmosphere in the cooling chamber has during the experiments had the same composition as the atmosphere in the nitrocarburizing furnace.
  • the nitrogen activity was similar, which reduces the risk for de-nitrification during the transport and quenching.
  • This atmosphere has had a main composition of nitrogen gas (N 2 ), hydrogen gas, (H 2 ), ammonia (NH 3 ), carbon monoxide (CO), carbon dioxide (CO 2 ) and in some cases small amounts of water (H 2 O).
  • the basic material can be varied. Experiments have been performed on steels of SS2541, SS2244, SS2142, SS2242 and SS1265, all of which have given a fully satisfactory result.
  • essentially all iron based steel materials can be treated by a nitriding process, comprising but not limited to carbon steels, low-alloyed steels, engineering steels, hardening and temper steels, case hardened steels, tool steel, stainless steel, precipitation hardening steels/Stainless steels and other steel variants.
  • Pre-oxidation temperatures in the interval of 300°C to 450°C are common in the technical field of nitriding, and are basically selected in dependence of the steel quality that is to be treated. For some materials, pre-oxidation is, however, not to recommend. However, the existence of a pre-oxidation step has no direct influence on the final quenching-coating operation.
  • nitriding process gas mixtures during the nitriding process can be utilized.
  • a nitrocarburizing atmosphere of only ammonia and carbon dioxide is possible to use.
  • pure nitriding can also be performed.
  • An atmosphere of only ammonia can then be utilized, possibly with nitrogen gas mixed in.
  • an endogas mixed with ammonia can be used.
  • the process temperatures during the nitriding can be different. Nitrocarburization temperatures from 500°C to 620°C are used in standard nitrocarburization processes and gives a possibility to adapt the nitriding process to the selected basic material, i.e. the steel quality. For instance, nitrided layer thicknesses from a fraction of a micrometer up to 35 ⁇ m have been achieved, and this increase the possibility to tailor the properties of the final material.
  • the adaptation of gas mixtures, temperatures and processing times gives a possibility to control the nitriding for achieving particular types of nitrided surfaces.
  • the quenching step to follow can be performed on any nitrided or nitrocarburized surface. In particular, such surfaces may be entirely without compound zone, or with a pure ⁇ ' nitride if this is to prefer for the intended final application or substrate material type.
  • the nitrided steel article was immediately quenched in a reactive quenching oil.
  • Non-exclusive examples of tungsten carriers suitable for use in reactive quenching oil formulations include simple tungstates, thiotungstates, tungsten dithiocarbamates, tungsten dithiophosphates, tungsten carboxylates and dithiocarboxylates, tungsten xanthates and thioxanthates, polynuclear tungsten complexes containing carbonyl, cyclopentadienyl and sulfur as ligands, halogen containing complexes of tungsten with pyridine, bipyridine, nitriles and phosphines as ligands, adducts of tunstic acid with fatty glycerides, amides and amines.
  • Known examples of commercial products suitable for this purpose include Vanlube W-324 from Vanderbilt International and Na-lube FM-1191 from King Industries.
  • Non-exclusive examples of molybdenum compounds suitable for use in reactive quenching oil formulations are simple molybdates, thiomolybdates, molybdenum dithiocarbamates, molybdenum dithiophosphates, molybdenum carboxylates and dithiocarboxylates, molybdenum xanthates and thioxanthates, polynuclear molybdenum complexes containing carbonyl, cyclopentadienyl and sulfur as ligands, halogen containing complexes of molybdenum with pyridine, bipyridine, nitriles and phosphines, adducts of molybdic acid with fatty glycerides, amides and amines.
  • Known examples of commercial products suitable for this purpose include Molyvan L and Molyvan 855 from Vanderbilt International, and Na-lube FM-1187 from King Industries.
  • Non-exclusive examples of boron compounds suitable for use in reactive quenching oil formulations are dispersed boric acid, dispersed metal borates, adducts of boric acid with amines and aminoalcohols, borate esters and ionic liquids containing boron cluster anions.
  • Known examples of commercial products suitable for this purpose include Vanlube 289 from Vanderbilt International, and Na-lube FM-1187 from King Industries.
  • Non-exclusive examples of sulfur compounds suitable for use in reactive quenching oil formulations are elementary sulfur or a variety of oil soluble organic sulfur compounds, the so-called sulfur carriers, including but not limited to sulfurized hydrocarbons, sulfurized fatty acids and sulfurized esters.
  • Non-exclusive examples of phosphorus compounds suitable for use in reactive quenching oil formulations are phosphoric acid triesters, such as tricresylphosphate, amine-neutralized mixtures of mono- and dialkyl phosphoric acid partial esters, ethoxylated mono- and dialkylphosphoric acids, dialkyl dithiophosphates, etc.
  • a naphthenic base oil T22 from Nynas Petroleum was used in combination with a universal quench oil additive package, OLOA 4751, from Oronite, used at treat levels between 1 to 10% of weight, and molybdenum phosphothioate, used at treat levels between 1 and 20% of weight in different tests.
  • OLOA 4751 from Oronite
  • molybdenum phosphothioate used at treat levels between 1 and 20% of weight in different tests.
  • Fatty triglyceride Plasmoil MR-A from Micros Lubrication Technologies, was added in concentrations of up to 10% of weight to boost dispersancy and to improve wetting.
  • Dialkyl polysulfide, Additin RC 2540 was added in amount up to 10% of weight to provide an additional source of S.
  • Zinc dithiophosphate, OLOA 262, from Oronite was used in concentrations up to 5% of weight to reduce the oxidation of the quenching oil and to provide an additional source of S and P.
  • the main purpose of these extra additives is to prolong the life time of the quenching oil, with no decisive effect on the formation of the solid lubricant layer.
  • Fig. 4 is a diagram illustrating the surface compositions for one sample quenched in a reactive oil and a similar sample quenched in a conventional oil.
  • the surface composition was analyzed using X-ray fluorescence measurements. It is easily noticed that the chemical surface composition of specimen processed using the reactive quenching method is very different from that for specimen processed using the conventional method.
  • the concentration of doping elements such as S, Zn and Mo are below the detection limit in the case of the conventional quenching.
  • FIG. 5 is a diagram illustrating coefficients of friction (COF) for different rotational speed for surfaces quenched in a reactive quenching oil according to the above presented compositions, compared with surfaces quenched in a conventional manner. It can easily be concluded that reactive quenching produces surfaces with a lower coefficient of friction as compared to the conventional quenching method.
  • the presented data are obtained in a lubricated friction test contact with a cross-cylinder configuration test specimen - probe arrangement at different specimen rotation speeds. The initial Hertzian contact pressure was around 1 GPa.
  • the steel articles produced by reactive quenching using at least one of S, P, B, Mo and W thus present a surface layer of a solid lubricant comprising at least one of S, P, B, Mo and W.
  • Fig. 6 illustrates schematically a cross-section of a portion of such a nitrided steel article 100.
  • the bulk metal alloy is a steel 102 corresponding to the original steel article before the nitriding step.
  • the heat treatment may change the metal phases of the original steel article, but with a same composition.
  • a nitrided layer 110 or boundary layer has been formed, in this article consisting of two zones 114 and 116.
  • a diffusion layer 116 or nitrogen diffusion zone forms the transition to the bulk material 102.
  • a compound layer 114 or nitrogen compound zone comprises typically a nitride/carbonitride mainly of the hexagonal epsilon phase.
  • the average nitrogen concentration increases towards the surface for a freshly nitrided product.
  • the boundaries between the zones are typically not sharp, but are instead a gradual transition from one layer constitution to another.
  • the nitrogen concentration increases typically from the bulk 102 of the steel article 100 towards the surface, as schematically indicated by the diagram at the right side of Fig. 5 .
  • the surface layer of a solid lubricant 120 bonds directly to the nitrided layer 110, and in this particular article to the compound layer 114.
  • the solid lubricant is chemically bonded directly to a freshly provided surface portion of the nitride layer having a highest nitrogen content.
  • the nitrided layer additionally comprises an outer zone, which typically comprises iron oxide and takes the effect of a passive layer.
  • an outer zone typically comprises iron oxide and takes the effect of a passive layer.
  • solid lubricants based on P and/or B may advantageously be used on such surfaces.
  • the nitriding step can be performed according to other nitriding processes, known as such in prior art.
  • the details of these alternative nitriding processes do not influence the solid lubricant coating in any decisive manner, and are thus not described in more detail here.
  • the nitrided layer may in such articles comprise e.g. only a nitrogen diffusion zone or only a nitrogen diffusion zone and a nitrogen compound zone.
  • the quenching speed and the concentrations of doping elements (S, P, B, Mo, W) in the quenching oil put some restrictions to the thicknesses of the solid lubricant that can be achieved.
  • a too thick solid lubricant layer may in certain applications be disadvantageous.
  • the concentrations in the oil of the substances to react and/or the time the steel article has a temperature high enough to cause a formation of the solid lubricant layer typically set some limitations on the maximum layer thickness. It is presently believed that it is preferred to have the layer of the solid lubricant with a thickness not exceeding a few ⁇ m.
  • the present invention is applicable to many kinds of articles.
  • Some nonlimiting examples are gears, crankshafts, camshafts, racks, pinions, axles, races, drive shafts, center pins and cylinder blocks for hydraulic motors, vanes for pumps, piston skirts, chain components, slideways, cam followers, valve parts, extruder screws, die-casting tools, forging dies, extrusion dies, firearm components, injectors, plastic-mold tools, conveyor guides, etc.
  • Fig. 7A illustrates schematically an example of an apparatus 1 for manufacturing of steel articles 100.
  • the apparatus 1 comprises a nitriding chamber 10.
  • the nitriding chamber 10 is configured for nitriding a steel article 100 at a nitrification temperature in the interval 350-650°C, giving a nitrided steel article.
  • the nitriding chamber 10 comprises an inlet valve 18, through which the steel articles 100 are entered and positioned on a holder 15.
  • Heater elements 14 are provided in the nitriding chamber 10 for providing the required temperatures.
  • a number of gas inlets 12 are provided, and the provision of gas is controlled in dependence of the required gas atmosphere inside the nitriding chamber 10.
  • the atmosphere inside the nitriding chamber 10 is successively changed and gas is therefore allowed to exit the nitriding chamber through a gas outlet 17.
  • the gas inlets 12, the gas outlet 17 and the heater elements 14 are preferably controlled based on sensors (not shown) surveilling the temperature and atmosphere composition inside the nitriding chamber 10.
  • the quenching volume 20 comprises reactive quenching oil 150 comprising at least one of S, P, B, Mo and W.
  • Gas inlets 36 to the quenching volume 20 ensures that an atmosphere in the quenching volume 20 has a nitrogen activity sufficient to mitigate de-nitrification of the steel articles 100. Typically, nitrogen gas is added.
  • Conveyor means 30 are provided for moving the nitrided steel articles 100 relative to said quenching volume comprising reactive quenching oil.
  • a horizontal translation means 32 is arranged for entering through the outlet valve 16, mechanically connecting to the holder 15 and retracting back to the quenching volume 20.
  • the outlet valve 16 may thereafter close in order to protect the nitriding chamber 10 for gases and liquids emitted from the reactive quenching oil 150 during quenching.
  • a vertical translation means 34 of the conveyor means 30 continues the moving of the steel articles 100 and by a vertical translation, the steel articles 100 are quenched in the reactive quenching oil 150.
  • the conveyor means 30 thereby moves the steel articles 100 when still having the nitrification temperature, and allows the nitrided steel articles 100 to be quenched in the reactive quenching oil 150 of the quenching volume 20.
  • This quenching results in that a solid lubricant comprising at least one of S, P, B, Mo and W is formed on the nitrided steel article.
  • the conveyor means 30 is thus arranged for moving the nitrided steel article 100 in an atmosphere of a nitrogen potential prohibiting de-nitriding an entire distance between the nitriding chamber 10 and the quenching volume 20.
  • the conveyor means 30 is arranged for moving the nitrided steel article 100 at the nitrification temperature an entire distance between the nitriding chamber 10 and said quenching volume 20.
  • the nitriding chamber 10 may have only one valve, both for introducing and removing the steel articles 100 from the nitriding chamber 10.
  • Fig. 7B illustrates schematically another apparatus 1 for manufacturing of steel articles 100.
  • the quenching volume 20 is situated beneath the nitriding chamber 10.
  • the conveyor means 30 are here adapted for moving the steel articles 100 vertically into the quenching oil 150.
  • a quenching oil for provision of a solid lubricant layer onto steel articles comprises a base oil and additives comprising at least one of S, P, B, Mo and W.
  • the quenching oil comprises S and at least one of Mo and W.
  • mineral-based oils are preferably used in formulations: from 100N for cold quench to 600N for hot quench. Accordingly, lower viscosities oils, such as T22 (Nynas), SN100 or SN200 (Total), are more suitable for cold quench with accelerated or medium cooling, while heavier products, such as SN500 (Total) or T100 (Nynas) are more suitable for hot quench with accelerated cooling.
  • quench oil The most important properties of quench oil are viscosity (ASTM D 445), flash point (ASTM D 92 or D93), water content (ASTM D 6304), acid number (ASTM D 664), precipitation number (ASTM D 91), metal content (ASTM D 4951 or D6595) and GM quenchometer (ASTM D 3520) or cooling curve analysis (ASTM D 6200). Cooling curve analysis allows easy detection of changes in the cooling rate due to oil oxidation or water contamination. Within certain limits, cooling curve can be "corrected" by using additives.
  • the additivation strategy is typically invariable with respect to temperature and aims for providing an oil that is more stable during the quenching process.
  • the most common additives being phenolic and aminic antioxidants, total base number buffering and detergency additives including calcium sulphonates, phenates, and ashless aminic, hydrocarbyl substituted succinic esters, amides and imides.
  • Such additivation is, as such, known in prior art, e.g. from the US patents US 6,239,082 or US 7,358,217 .
  • Non-exclusive examples of known commercial packages are OLOA 4750, OLOA 4751 from Oronite and LZ 5357 from Lubrizol.
  • the quenching oil comprises these quench oil additives in an amount of at most 10% of weight.
  • a further particular example of a quench oil that advantageously has been used for reactive quenching can be composed according to: Universal quench oil additive package, Lubrizol 5357S 4 to 6% Tungsten thiocarbamate 1 to 10% Base oil, NS 100 the rest
  • a quench oil that advantageously has been used for reactive quenching can be composed according to: Universal quench oil additive package, Lubrizol 5941S 2 to 6% Antioxidant Irganox L150 0.1 to 0.5% Antioxidant DBDS 0.1 to 0.5% Borate ester Vanlube 289 1 to 10 % Base oil, T 110 the rest

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Claims (3)

  1. Verfahren zur Herstellung von Stahlartikeln, umfassend die Schritte des:
    Nitrierens (210) eines Stahlartikels bei einer Nitrifizierungstemperatur im Bereich von 350-650 °C;
    wobei der Schritt des Nitrierens eines Stahlartikels zu einem nitrierten Stahlartikel führt; und
    Abschreckens (220) des nitrierten Stahlartikels in einem Abschrecköl von der Nitrifizierungstemperatur,
    dadurch gekennzeichnet, dass
    das Abschrecköl ein reaktives Abschrecköl ist, das eine oder mehrere oberflächenreaktive Verbindungen enthält, die als Träger mindestens eines von S, P, B, Mo und W dienen;
    wobei der Schritt des Abschreckens zusätzlich Beschichten (222) des nitrierten Stahlartikels durch ein festes Schmiermittel umfasst, das mindestens eines von S, P, B, Mo und W umfasst;
    wobei das reaktive Abschrecköl mindestens 0,1 Gew.-% der Gesamtheit von S, P, B, Mo und W umfasst;
    wobei das reaktive Abschrecköl höchstens 10 Gew.-% der Gesamtheit von S, P, B, Mo und W umfasst;
    und durch den weiteren Schritt des:
    Haltens des nitrierten Stahlartikels in einer Atmosphäre eines Stickstoffpotentials, das die Entstickung während einer gesamten Zeitspanne zwischen dem Schritt des Nitrierens (210) und dem Schritt des Abschreckens (220) verhindert.
  2. Verfahren nach Anspruch 1, gekennzeichnet durch den weiteren Schritt des Haltens des nitrierten Stahlartikels bei der Nitrifizierungstemperatur während einer gesamten Zeitspanne zwischen dem Schritt des Nitrierens (210) und dem Schritt des Abschreckens (220).
  3. Verfahren nach Anspruch 1 oder 2, dadurch gekennzeichnet, dass der Schritt des Abschreckens (220) mit einer maximalen Kühlgeschwindigkeit von weniger als 250 °C/s ausgeführt wird.
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